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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059156, TK2
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
+2 more
GUncertain significance
LOC130059156, TK2
(P41H)
Single nucleotide variant
(intron variant +3 more)
Mitochondrial DNA depletion syndrome, myopathic form
+2 more
GConflicting classifications of pathogenicity
LOC130059156, TK2
(R32W)
Single nucleotide variant
(missense variant +3 more)
not provided
+3 more
GBenign/Likely benign
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